Senior Clinical Data Associate

Requisition ID: 12339Position Title: Senior Clinical Data AssociateWorking Location: Cambridge, MARequired Experience: See DescriptionRequired Education: See DescriptionRequired Travel: 0Job DescriptionGenzyme Corporation, ranked as one of the foremost biotechnology companies in the world, is committed to providing an exceptional environment in which individuals can excel, and achieve their professional and personal goals. Genzyme Corporation has been selected by FORTUNE magazine as one of the "100 Best Companies to Work For in 2007 in the United States”. By applying for a position with Genzyme, you are taking the first step toward becoming a part of our dynamic and talented team, and sharing in our continued success.Genzyme Corporation currently has an immediate need for an experienced Senior Clinical Data Associate (CDA) based in our Cambridge, MA headquarters. Responsibilities include:Design of eCRF and Case Report Forms, data conventions and databases according to SOPs, protocols and project team specifications. Development of project specific guidelines. Assistance with training in data management procedures. Review of clinical data to ensure consistency, integrity, and accuracy using project specific guidelines. Review of clinical data using adhoc retrievals (i.e., SQL); queries investigational sites regarding omissions, errors, or inconsistencies. Creation of queries resulting from coding of data, including adverse events, diagnoses, surgical procedures, etc., using standard international dictionaries. Work with project managers to determine, review and execute appropriate data management practices for each project assigned. Assist with developing project timelines and ensures ongoing transmissions of data. Prioritize tasks with respect to timelines. Interact with external laboratories and contract research organizations to ensure that appropriate laboratory evaluations are scheduled, and that all data related activities are performed according to protocol, GCP and approved SOPS. Follow established procedures. Work is performed under general direction. The Sr CDA will work independently to determine and develop approach to solution. Work is reviewed for soundness of technical judgment and overall adequacy and accuracy. EDC experience preferred. Frequent inter-organizational and outside customer contacts. Represents the organization in providing solutions to difficult technical issues associated with clinical trial projects.Basic Qualifications: Bachelor's Degree in life sciences and 4 years experience in clinical trials or Master's Degree and 3 years experience..